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nsv6763975

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,373

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 143 SVs from 30 studies. See in: genome view    
    Submitted genomic79,243,387-79,257,759Question Mark
    Overlapping variant regions from other studies: 143 SVs from 30 studies. See in: genome view    
    Remapped(Score: Perfect):78,539,210-78,553,582Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6763975Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr579,243,38779,257,759
    nsv6763975RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr578,539,21078,553,582

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18517805deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18517805Submitted genomicNC_000005.10:g.792
    43387_79257759del
    GRCh38 (hg38)NC_000005.10Chr579,243,38779,257,759
    nssv18517805RemappedPerfectNC_000005.9:g.7853
    9210_78553582del
    GRCh37.p13First PassNC_000005.9Chr578,539,21078,553,582

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv185178051.4e-054276252
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